RS886041053 TRAPPC11

Health Risk Chr 4:183686751
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What This Variant Does
"CLNSIG=5
Associated Conditions
Autosomal recessive limb-girdle muscular dystrophy type R18
Autosomal recessive limb-girdle muscular dystrophy type R18
Other Variants in TRAPPC11
rs397509417 rs397509418 rs151021715 rs886041052 rs780139133 rs150331292 rs148833310 rs111381550 rs769785004 rs1554009901
Ask Dr. Hemsworth about this variant